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首页> 外文期刊>Immunology Letters >Effective inhibition of a Strongylocentrotus nudus eggs polysaccharide against hepatocellular carcinoma is mediated via immunoregulation in vivo.
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Effective inhibition of a Strongylocentrotus nudus eggs polysaccharide against hepatocellular carcinoma is mediated via immunoregulation in vivo.

机译:通过体内免疫调节来介导对猪圆核裸球虫卵多糖的有效抑制以抵抗肝细胞癌。

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This study was aimed at evaluating the inhibitory effect of a polysaccharide that was isolated from Strongylocentrotus nudus eggs (SEP) against hepatocellular carcinoma in H22-bearing mice and elucidating its immunological mechanisms by determining its effects on the growth of transplanted tumors and immune response in H22-bearing mice. ICR mice inoculated with mouse hepatoma carcinoma cell lines H22 were treated with SEP at doses of 4, 8, 16 mg/kg/d for 12 days. The effects of SEP were measured via the growth of the transplanted tumors, splenocyte proliferation, T lymphocytes counts, CTL activity, the production of cytokines from splenocytes and the levels of serum Ig in tumor-bearing mice. In addition, the effects of SEP on Erk phosphorylation in mouse splenocytes and on the transcriptional activity of NFAT in Jurkat T cells were also investigated. Our results showed that SEP significantly inhibited the growth of transplanted tumors in mice. SEP could not only remarkably enhance splenocyte proliferation, CD4(+) and CD8(+) T cell numbers as well as CTL activity, but it also elevated IL-2 and TNF-alpha secretion as well as IgA, IgM and IgG levels in the serum. Furthermore, the activation of Erk phosphorylation and the NFAT promoter by SEP promoted the transcription and expression of downstream gene IL-2. In conclusion, our study demonstrates that SEP effectively inhibits hepatocellular carcinoma in vivo via enhancement of host immune system function, and it could be a potential therapeutic drug for hepatocarcinoma.
机译:这项研究的目的是评估从圆支原体卵(SEP)分离出的多糖对荷H22小鼠肝细胞癌的抑制作用,并通过确定其对移植瘤生长和H22免疫应答的作用来阐明其免疫学机制。的小鼠。用SEP以4、8、16 mg / kg / d的剂量对接种了小鼠肝癌细胞H22的ICR小鼠进行12天的治疗。通过移植肿瘤的生长,脾细胞增殖,T淋巴细胞计数,CTL活性,脾细胞产生的细胞因子的产生以及荷瘤小鼠血清Ig的水平来测量SEP的作用。此外,还研究了SEP对小鼠脾细胞Erk磷酸化以及Jurkat T细胞中NFAT转录活性的影响。我们的结果表明,SEP显着抑制小鼠移植肿瘤的生长。 SEP不仅可以显着增强脾细胞增殖,CD4(+)和CD8(+)T细胞数量以及CTL活性,而且还可以提高IL-2和TNF-α分泌以及IgA,IgM和IgG水平。血清。此外,SEP对Erk磷酸化和NFAT启动子的激活促进了下游基因IL-2的转录和表达。总之,我们的研究表明SEP可通过增强宿主免疫系统功能有效地抑制体内肝细胞癌,并且它可能是肝癌的潜在治疗药物。

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